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(HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2

Base Information
  • Chemical Name:(HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2
  • CAS No.:269727-14-2
  • Molecular Formula:C36H35B3N4O9
  • Molecular Weight:698.689
  • Hs Code.:
(HO)2<sup>(10)</sup>BC<sub>6</sub>H<sub>4</sub>CH<sup>(15)</sup>NOC<sub>6</sub>H<sub>4</sub>CH<sub>2</sub>N(CH<sub>3</sub>)CH<sub>2</sub>C<sub>6</sub>H<sub>3</sub>(ONCHC<sub>6</sub>H<sub>4</sub><sup>(10)</sup>B(OH)2)2

Synonyms:

Suppliers and Price of (HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2
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Chemical Property of (HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2
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Technology Process of (HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2

There total 7 articles about (HO)2(10)BC6H4CH(15)NOC6H4CH2N(CH3)CH2C6H3(ONCHC6H4(10)B(OH)2)2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trifluoroacetic acid; In dimethyl sulfoxide; solns. of formylboronic acids in DMSO mixed in equal vols.; 1% CF3CO2H added; added to aminooxy compd. soln. (stoichiometry: 1.25 equiv. of formylboronic acid per aminooxy group); 24 h; further products; without isolation; detd. by mass spectrometry;
DOI:10.1021/ja993844v
Guidance literature:
With trifluoroacetic acid; In dimethyl sulfoxide; solns. of formylboronic acids in DMSO mixed in equal vols.; 1% CF3CO2H added; added to aminooxy compd. soln. (stoichiometry: 1.25 equiv. of formylboronic acid per aminooxy group); 24 h; further products; without isolation; detd. by mass spectrometry;
DOI:10.1021/ja993844v
Guidance literature:
With trifluoroacetic acid; In dimethyl sulfoxide; solns. of formylboronic acids in DMSO mixed in equal vols.; 1% CF3CO2H added; added to aminooxy compd. soln. (stoichiometry: 1.25 equiv. of formylboronic acid per aminooxy group); 24 h; further products; without isolation; detd. by mass spectrometry;
DOI:10.1021/ja993844v
upstream raw materials:

(HO)2(10)BC6H4CHO

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